تفاعل #569763

ord-32e8c57ec5c049ef920a87f0f4f3c39d

معادلة التفاعل

NCCCCN1CCCCC1
1-(4-aminobutyl)piperidine
O=C(O)c1n[nH]c2ccccc12
1H-indazole-3-carboxylic acid
O=C(n1ccnc1)n1ccnc1
1,1'-carbonyldiimidazole
O=C(NCCCCN1CCCCC1)c1n[nH]c2ccccc12
oil
المردود 101.3%
O=C(NCCCCN1CCCCC1)c1n[nH]c2ccccc12
N-[4-(1-piperidinyl)butyl]-1H-indazole-3-carboxamide
المردود 101.3%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGThis solution was then stirred at room temperature for 18 h
  2. 2
    أخرىthe volatiles were evaporated
  3. 3
    workup.ADDITIONthe residue was diluted with water
  4. 4
    استخلاصExtraction with ethyl acetate

الإجراء التجريبي

To a solution of 1H-indazole-3-carboxylic acid (0.745 g, 4.6 mmol) in 20 mL dimethylformamide, was added 1,1'-carbonyldiimidazole (0.745 g, 4.6 mmol). This mixture was stirred at room temperature for 4 h, and to it was added dropwise a solution of 1-(4-aminobutyl)piperidine (0.718 g, 4.6 mmol) dissolved in 3 mL dimethylformamide. This solution was then stirred at room temperature for 18 h, the volatiles were evaporated and the residue was diluted with water. Extraction with ethyl acetate followed by water and brine washes gave 1.40 g of an oil which was sufficiently pure for use in the next reaction. Mass spectrum, m+ =301.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05798367uspto-grants-1998_08